Seed dormancy dynamics and germination characteristics of Solanum nigrum

Four experiments were conducted to study seed dormancy and germination requirements in Solanum nigrum . In Expt 1, seeds were stratified at different constant and stepwise rising temperatures and their germinability was tested at three germination regimes at weekly intervals. In Expts 2–4, seeds dry stored at 4°C and stratified at 5 and 15°C were tested at constant temperatures, as well as fluctuating temperatures with constant and increasing amplitudes. Results suggest that the rate of dormancy release increased with increasing temperatures ranging from 4.5 to 18.6°C. However, prolonged stratification at higher temperatures caused subsequent induction of dormancy. When tested at constant temperatures, stratified seeds germinated between 18 and 34°C, with the optimum between 26 and 30°C, while dry-stored seeds showed no germination. Fluctuating temperatures, with amplitudes ranging from 5 to 15°C, promoted germination of seeds from all treatments. The dormancy dynamics and germination characteristics of the species will have implications for its survival and establishment. This information can be used to predict time of emergence and, thus, improve control of the species in weed management systems.     

How much of seed dormancy in weeds can be related to seed traits?

Seed dormancy contributes to species persistence in unpredictable environments and is a key process to be taken into account in weed dynamics models. As the level of seed dormancy, photosensitivity and the dates of dormancy induction and release are difficult to measure, our objective was to relate weed seed dormancy with morphological, chemical or physiological seed traits and with expert knowledge. Dormancy of four species was studied experimentally during a 2‐year seed burial experiment. Experiments were supplemented with data from the literature to increase the number of species analysed, resulting in a data set of 29 species. Proportions of non–dormant seeds were higher for elongated than spherical seeds, even when accounting for phylogenetic relatedness between species. Elongated seeds, which tend to remain on the soil surface in undisturbed habitats, may have been selected for lack of dormancy and immediate germination to limit mortality due to predation. Dormancy increased with seed coat thickness, which can act as a chemical and physical barrier to germination, while no relation was found with seed lipid or protein content. No correlation was found between photosensitivity parameters and any of the species traits analysed. Variations in dormancy dates (induction and release) were highly correlated with average field emergence season estimated from expert knowledge. The observed correlations suggest that the level of dormancy results both from direct and from indirect effects of traits being involved in trade‐offs together with seed mortality.     

Seasonal changes in seed dormancy of Solanum nigrum and Solanum physalifolium

The seed dormancy cycle in Solanum nigrum and Solanum physalifolium was studied in relation to seasonal temperature. Seed lots of both species were buried in pots outdoors in a randomised complete block design with four replicates from November 2004 to November 2006. At regular intervals, samples of the seeds were randomly exhumed and tested for germination in incubators at three temperatures and light/darkness regimes. For both species, low winter temperature weakened dormancy and high temperature strengthened it. Dormancy induction mainly occurred from August to October in both species after experiencing warm temperatures. An exception from the general pattern of seed dormancy was however observed; seed germination percentages were temporarily reduced in early spring, followed by a peak in germination, before the main period of strong dormancy in S. nigrum . The same phenomenon was observed in S. physalifolium during June in the first year. This short-lived dormancy induction might explain the late emergence of the species. Seed dormancy enables the species to maximise its chance of survival by regulating germination timing to favourable conditions. Therefore, information on the dormancy cycle can be used to predict seedling emergence and optimise weed control operations.     

How to model the effects of farming practices on weed emergence

Early weed emergence models directly relate the weed seedbank to emerged seedlings, with constant emergence rates for each tillage tool. These models compare cropping systems at long term in a given region. Other models relate emergence to rain and air temperature. They are useful in no-till systems with seeds close to soil surface. Recently, other authors split emergence into germination and pre-emergence growth, depending on soil climate. But seed survival and dormancy as well as tillage were not yet integrated. Models advising farmers for strategic farming decisions in a large range of situations must split emergence into mechanistic relationships distinguishing the various underlying biological subprocesses in order to correctly quantify the effect of cropping system. The model Alomy Sys for Alopecurus myosuroides emergence follows this principle, based on submodels predicting (a) soil environment resulting from the cropping system, (b) vertical soil seed distribution after tillage, and (c) seed survival, germination and pre-emergence growth depending on soil environment, seed depth, characteristics and past history. This model can be used to determine the optimal tillage modes and sowing dates, depending on the preceding crop succession, the following crop and the work constraints of the farmer.     

Germination, emergence, and dormancy of Mimosa pudica

Mimosa pudica (common sensitive plant) is a problematic weed in many crops in tropical countries. Eight experiments were conducted to determine the effects of light, seed scarification, temperature, salt and osmotic stress, pH, burial depth, and rice residue on the germination, seedling emergence, and dormancy of M. pudica seeds. Scarification released the seeds from dormancy and stimulated germination, though the germination of the scarified seeds was not influenced by light. The scarification results indicate that a hard seed coat is the primary mechanism that restricts germination. The germination increased markedly with the exposure to high temperature "pretreatment" (e.g. 150°C), which was achieved by placing non-scarified seeds in an oven for 5 min followed by incubation at 35/25°C day/night temperatures for 14 days. The germination of the scarified seeds was tolerant of salt and osmotic stress, as some seeds germinated even at 250 mmol L⁻¹ NaCl (23%) and at an osmotic potential of −0.8 MPa (5%). The germination of the scarified seeds was >74% over a pH range of 5–10. The seedling emergence of the scarified seeds was 73–88% at depths of 0–2 cm and it gradually decreased with an increasing depth, with no seedling emergence at the 8 cm depth. The rice residue applied to the soil surface at rates of ≤6 t ha⁻¹ did not influence the seedling emergence and dry weight. The information gained from this study identifies some of the factors that facilitate M. pudica becoming a widespread weed in the humid tropics and might help in developing components of integrated weed management practises to control this weed.     

Effect of soil moisture during stratification on dormancy release in seeds of five common weed species

Although the effects of cold stratification on the release of physiological dormancy in seeds have been studied extensively, knowledge of the role of soil moisture content on seed dormancy release during cold stratification is limited. Our study determined seed dormancy characteristics and the effect of soil moisture content on seed dormancy breakage during cold stratification in the five common weed species Amaranthus retroflexus, Chenopodium album, Chenopodium hybridum, Plantago lanceolata and Setaria glauca. Seeds of all five species were dormant at the time of harvest and their germination response to light and temperature varied. Soil moisture content had a significant effect on seed dormancy release of all species except P. lanceolata. Germination percentage of A. retroflexus, C. album, C. hybridum increased and then decreased as soil moisture content increased, regardless of germination test temperature. The optimal soil moisture content and seed moisture content for dormancy breakage of A. retroflexus, C. album, C. hybridum were 8%, 12%, 8% and 22.0%, 37.7%, 25.7% respectively. Dry storage (after‐ripening) significantly increased germination of S. glauca. Moreover, increasing soil moisture content first slowed and then increased dormancy breakage in S. glauca. These results suggest that data on soil moisture content should be incorporated into models that predict weed seed dormancy breakage and timing of seedling emergence as well as those for weed management.     

Light, temperature and burial depth effects on Rumex obtusifolius seed germination and emergence

Trials were carried out to investigate the effects of light and temperature on germination of Rumex obtusifolius L. After several months of storage, seeds gradually lost dormancy and became photosensitive. Thermal optima for germination were between 20 °C and 25 °C in light or in darkness. At lower temperatures there was a greater demand for light, so that the greatest differences in germination percentage (between low and high temperatures) were found within the 10–15 °C temperature range. The calculated thermal minima ( x -intercept method) in light and darkness were 8.3 °C and 6.1 °C respectively. Daily temperature fluctuation increased germination even after seed irradiation with far-red light, suggesting a lower demand for the far-red-absorbing form of phytochrome. Seed burial inhibited germination in proportion to depth; however, germination inhibition was independent of seed phytochrome photo-equilibrium, which had been diversified by seed pretreatment with light. Seedlings did not emerge when seeds were buried >8 cm deep. Recovery of ungerminated seeds showed that excessive burial did not impede seedling emergence but rather prevented seed germination. However, this induction of dormancy was lost once germination processes were activated (24–48 h at 20 °C) that made germination irreversible. Temperature was also involved in inhibition, and low temperature (<15 °C) induced the least inhibition. This is discussed in terms of processes of respiration and fermentation in buried seeds.     

Digitaria sanguinalis seed dormancy release and seedling emergence are affected by crop canopy and stubble

Digitaria sanguinalis is a troublesome annual weed that causes important yield losses in different crops. Despite this, there is scarce information about different aspects of its biology under field conditions. New knowledge about the establishment process of this species will be of paramount importance in order to maximise the effectiveness of weed management. The aims of this paper were to evaluate the effect of stubble found on the surface on seed dormancy levels through the season, the effects of stubble and soyabean crop canopy on seedling emergence and to determine the field emergence pattern as a consequence of seed dormancy level at dispersal time. Seeds on the soil surface, which showed a high dormancy level at the beginning of autumn, were released from dormancy by low winter temperatures and germinated during spring as temperatures rose, showing a transient surface seedbank. Seeds covered by stubbles had delayed the emergence in the field due to lower alternating temperatures perceived by the surface seedbank. On the other hand, the presence of a soyabean crop and stubble together reduced the number of seedlings. Seeds with a high dormancy level at dispersal time showed a delayed emergence in the next season when compared with seeds with a lower dormancy level. However, the final number of seedlings was similar. Both stubble on surface and crop canopy are useful factors to lessen and delay the seedling emergence allowing the design of weed management strategies in order to diminish the population levels of this species.     

Emergence of Chenopodium album and Stellaria media of different origins under different climatic conditions

Summary The emergence behaviour of weed species in relation to cultural and meteorological events was studied. Dissimilarities between populations in dormancy and germination ecology, between-year maturation conditions and seed quality and burial site climate all contribute to potentially unpredictable variability. Therefore, a weed emergence data set was produced for weed seeds of Stellaria media and Chenopodium album matured and collected from three populations (Italy, Sweden and UK). The seeds were collected in two consecutive seasons (1999 and 2000) and subsequently buried in the autumn of the same year of maturation in eight contrasting climatic locations throughout Europe and the USA. The experiment sought to explore and explain differences between the three populations in their emergence behaviour. Evidence was demonstrated of synchrony in the timing of the emergence of different populations of a species at a given burial site. The relative magnitudes of emergence from the three populations at a given burial site in a given year were generally similar across all the burial sites in the study. The resulting data set was also used to construct a simple weed emergence model, which was tested for its application to the range of different burial environments and populations. The study demonstrated the possibility of using a simple thermal time-based model to describe part of the emergence behaviour across different burial sites, seed populations and seasons, and a simple winter chilling relationship to adjust for the magnitude of the flush of emergence at a given burial site. This study demonstrates the possibility of developing robust generic models for simple predictions of emergence timing across populations.     

Annual cycles of germinability and differences between primary and secondary dormancy in buried seeds of Echinochloa crus-galli

The seasonal changes in percentage of dormant seeds of Echinochloa crus-galli in the field were recorded for 4 years. The lots of seeds were wrapped in nylon fabric, buried 20 cm under the grass sward and exhumed at monthly intervals. The proportion of seeds germinating under light conditions at a constant temperature of 25 °C fluctuated between 0% and 96%, with maxima in May–July and minima in September–November. Small between-year differences in the course of summer dormancy induction and its winter termination were probably caused by variation of weather conditions.
Attributes of dormancy innate to seeds after maturation (primary dormancy) and dormancy induced in buried seeds during the summer (secondary dormancy) were compared by investigating the rate of dormancy termination during storage of (a) dry seeds at 25 °C, (b) imbibed seeds at 5°C and (c) in seeds buried under field conditions during October–June. Percentage of germination increased faster in secondary than primary dormant seeds at both constant 25 °C and 5 °C. The seeds with primary and secondary dormancy also differed in the response to `germination pre-treatment', a 10-day exposure of imbibed seeds at 25 °C that causes germination of the non-dormant fraction of seed materials. After this treatment the time to resuming germination in primary dormant seeds was substantially increased, whereas the secondary dormant seeds were much less affected. Annual variation in the proportion of germinable seeds explains the low efficiency of autumn soil cultivation for decreasing reserves of E. crus-galli seeds in the soil.     

Seasonal changes in the germination of buried seeds of Monochoria vaginalis

This study investigates the seasonal variation of germination ability of buried seeds of Monochoria vaginalis (Burm.f.) Presl var. plantaginea Solms. The field-collected seeds were buried in a flooded or an upland field and then exhumed monthly. The exhumed seeds were germinated under four temperature regimes. The seeds exhumed from the flooded soil were dormant at the beginning of burial and proceeded into a conditional dormancy/non-dormancy/conditional dormancy cycle throughout the remaining period of the experiment. The seeds exhumed monthly from the non-flooded soil exhibited an annual dormant cycle, which is dormancy/conditional dormancy/non-dormancy/conditional dormancy/dormancy. At day and night temperatures of 25/20 °C, the exhumed seeds from both the flooded and the upland soil resembled each other in terms of seasonal variation of the germination percentage. In September and October, more seeds exhumed from upland soil failed to germinate under higher temperature than from flooded soil. Strictly avoiding exposure to light during seed exhuming and seed testing prevented the seeds from germinating. A short exposure of the exhumed seeds to light during preparation promoted dark germination when the seeds were at the non-dormant stage. The potential implications of our results for weed management strategies in rice production are discussed.     

Modelling Chloris virgata germination and emergence under different temperature and light quality conditions

Chloris virgata is a problematic weed around the world. Prediction of weed germination rates could be a useful strategy to optimise timing of weed control actions. We studied the germination and emergence of C. virgata collected seeds under different after-ripening treatments and different exhumation dates after seed dispersal, to estimate seed dormancy level and predict weed emergence dynamics under field conditions. Three experiments were conducted under controlled conditions to determine base, optimum and maximum germination temperatures (T_b, T_o and T_m respectively) and comprised: (a) exposure of seeds to gradually increasing and decreasing temperatures between 5 and 35°C; (b) exposure of seeds to different constant temperatures; and (c) exposure of seeds to different light quality conditions (red – far red ratio) and temperature regimes (constant and alternating temperatures). To explore genuine environmental conditions, a field experiment was performed to determine weed emergence under different shading levels. Finally, with the data obtained, a thermal time model for dormancy release was used to predict C. virgata seedling emergence in the Argentine Pampas region. Seeds after-ripened in cold and wet conditions and constant 25°C showed the highest germination percentages. The values of T_b (7°C), T_o (28°C) and T_m (40°C) remained constant at all exhumation dates. Neither light quality nor thermal regime modified the final germination percentages. However, shading delayed seedling emergence under field conditions, even when it was adjusted by thermal time. These results may allow predicting C. virgata emergence in temperate regions and help to improve weed control in integrated weed management strategies.     

不同贮藏条件下龙葵种子的季节性休眠特性

龙葵是农田恶性杂草?为明确龙葵种子休眠与季节温度的关系, 研究了室内和室外不同贮藏条件下其种子萌发对温度的响应规律?结果表明, 室外贮藏条件下的龙葵种子萌发呈季节性变化, 从10月到翌年5月, 龙葵种子萌发率均在95%以上, 随着夏季温度的升高, 萌发率从6月开始下降, 9月达到最低值(25.4%), 由此进行年际间休眠和非休眠周期的循环?夏季6月-9月的高温可诱导龙葵种子进入休眠状态, 而秋冬季的相对低温有利于解除种子休眠, 使种子恢复萌发状态?龙葵种子休眠和非休眠状态之间的切换受季节性温度变化的影响?室内贮藏的种子, 由于环境温度较为稳定, 其萌发率年际变化较小, 在20%~50%之间?本文明确了龙葵种子休眠的周期性变化规律, 有助于精准预测其出苗时间, 研究结果可为阐明龙葵种子休眠萌发机制和制订基于萌发调控的绿色防控策略提供依据?     

Dormancy,germination and emergence of Urochloa panicoides regulated by temperature

Urochloa panicoides is an annual weed of summer crops. In Argentina, in subhumid areas with monsoon rainfall, it germinates and establishes in a single flush. To (i) identify the environmental factors that modify its seed dormancy level and germination and (ii) quantify the parameters describing the thermal behaviour of the germination and emergence dynamics of this weed under non‐limiting water conditions, we established a set of germination experiments performed (i) under controlled conditions using seeds after ripened for 3 or 6 months in different thermal and hydric conditions and (ii) under field conditions, where the soil temperature was modified by applying different shading levels. Seed dormancy level remained high with 3 months after ripening in all treatments. After 6 months, seeds stored at 4°C in dry conditions did not germinate at any temperature, while seeds stored at 25°C in dry conditions and in situ germinated c. 20% and 60% respectively. Germination percentage was higher in seeds harvested before their natural dispersal. The base, optimum and maximum temperatures for seed germination were 6, 35 and 45°C respectively. Shading reduced the number of emerged seedlings, possibly by reducing the soil thermal amplitude. The results explained the dormancy‐breaking mechanism of U. panicoides that allows a high germination rate in the field when rainfall occurs.     

Germination ecology of Leptochloa chinensis: a new weed in the Italian rice agro-environment

Leptochloa chinensis is a new weed that has been found with increasing frequency in Italian rice paddies. The germination ecology of L. chinensis seeds was studied in order to investigate the development mechanisms and survival strategy of this weed in rice paddies of northern Italy. Leptochloa chinensis seeds showed no dormancy and exhibited germination even in anoxic conditions. Germination was strongly influenced by temperature (minimum around 15°C; optimal 25–35°C) and light (phytochrome dependent). Temperature fluctuation caused an increase of seed germination in the dark. Seed burial also strongly inhibited germination and emergence of this species. At 5 cm seed burial only 5% of seedlings emerged in flooded conditions, while at the same depth, but with no flooding, no seedling emergence was observed. This phenomenon was not due to oxygen depletion, as germination was not inhibited by complete anoxia, as demonstrated by the fact that some seedlings did emerge in flooding conditions when water was no deeper than 6 cm. Seed burial and concomitant flooding induced an unusual germination: first coleoptile emergence and subsequently emergence of the radicle was observed. The possible exploitation of this knowledge for weed management is discussed.     

Biology of Commelina benghalensis L. in south-eastern Queensland. 2. Seed dormancy, germination and emergence

Germination of freshly harvested seeds of Commelina benghalensis L. varied from 0–3% for small aerial seeds, 20–35% for large aerial seeds and from 33% for small underground seeds to 90% for large underground seeds. Innate dormancy of all seed types was completely overcome by clipping the seed coat. Exposure to 90°C dry heat for 2 h was also effective in increasing germination of the three strongly dormant seed types. Optimum temperature for germination varied with the different seed types. Periods of likely major weed infestation from the four seed types were predicted using soil temperature data. Exposure to light increased germination but was not essential and underground seeds responded more to light than aerial seeds. Optimum depth of emergence for the four seed types was from 0 to 50 mm and there was a positive correlation between maximum depth of emergence and seed weight.     

Weed seed rain interception by grass cover depends on seed traits

Weed management requires a better understanding of the dynamics of the weed seedbank, which is a primary source of weeds in a field. Seeds reaching the ground after seed rain replenish the seedbank and therefore contribute to future weed infestations. Our investigation is based on the hypothesis that a permanent vegetation cover, such as a grassland, can prevent weed seeds from reaching the ground. Therefore, we developed an innovative experimental device to simulate in controlled conditions the seed rain of 12 weed species (Capsella bursa‐pastoris, Conyza canadensis, Myosotis arvensis, Papaver rhoeas, Poa annua, Polygonum aviculare, Ranunculus sp., Rumex obtusifolius, Sonchus asper, Stellaria media, Taraxacum officinale and Veronica persicaria). We quantified the interception of weed seeds by a grass cover. Grass cover height, seed size and seed appendage (e.g. pappus, wing or awn) increased seed interception, in contrast to seed weight and shape index. From these results, we established a linear model to predict weed seed interception by a grass cover as a function of their seed trait values. The relationship between the predicted interception and weed community dynamics observed in grasslands was negative for some species, indicating that other processes may be involved depending on weed species. The weed seed interception model will be incorporated into an existing model of weed population dynamics to simulate the impact of grassland insertion into arable crop rotations.     

Variation in seed dormancy and light sensitivity in Alopecurus myosuroides and Apera spica-venti

Variation in seed dormancy and light sensitivity was studied in Alopecurus myosuroides and Apera spica-venti . Seeds were collected from different populations, at different dates and from plants emerging in autumn or spring, and used in four experiments. In the first experiment, initial dormancy was investigated in light and darkness. In Expt 2, buried seeds were exhumed on 16 occasions, from September 1997 to March 2000, and germinated in light, in darkness and after a 5-s light exposure. In Expt 3, emergence was recorded for seeds sown in pots outdoors. In Expt 4, stratified seeds of A. myosuroides only were exposed to photon irradiance ranging from 0.1 to 25 600 μmol m⁻². Variation was high among seed collections, but both species showed winter annual dormancy patterns. Apera spica-venti germinated to high percentages in autumn but negligibly in spring. Alopecurus myosuroides germinated less in spring when tested in darkness and after a short light exposure and emerged poorly in spring, which reflected photo-desensitisation during cold stratification. We conclude that the peak of emergence in A. myosuroides , and to some extent in A. spica-venti , is largely regulated by exposure to light interacting with low-level dormancy. This offers valuable information regarding optimal timing of weed control measures.     

Thermal and hormonal regulation of the dormancy–germination transition in Amaranthus tuberculatus seeds

The transition from seed dormancy to germination is a multi‐step process. However, distinguishing between physiological processes involved in seed dormancy alleviation and those involved in germination has been difficult. We studied the seed dormancy alleviation process in Amaranthus tuberculatus, an important weed species in midwestern USA. Using three A. tuberculatus biotypes that differ in dormancy level, it was determined that stratification reduced seed dormancy from a high to a low level. Temperature alternation alleviated low seed dormancy and triggered germination. Exogenously applied abscisic acid (ABA) and gibberellic acid (GA) had no effect on seeds with high dormancy. However, ABA and paclobutrazol (a GA biosynthesis inhibitor) significantly reduced germination of seeds with low dormancy. Hormones could not replace the effects of stratification or temperature alternation on dormancy alleviation. Based on our results, we propose a seed dormancy–germination transition model in which the dormancy of A. tuberculatus seeds is progressively reduced from a high to a low level; but environmental conditions (i.e. stratification) can accelerate the dormancy alleviation process. Under low dormancy levels, the seed is more sensitive to environmental cues that are responsible for removing dormancy and triggering germination (i.e. temperature alternation). Finally, ABA and GA regulation occurs primarily during the final transition from low dormancy to germination rather than the alleviation of high dormancy.     

Germination characteristics and emergence time of annual Bromus species of differing weediness in Sweden

The germination ecology of four annual Bromus species, which differ in weediness on arable land in southern Sweden, was investigated. The most problematic species is Bromus sterilis , while Bromus hordeaceus frequently occurs on arable land. In contrast, Bromus arvensis is a rare weed, and Bromus tectorum is found infrequently in fields despite being a widespread ruderal species. Five experiments were conducted to identify germination characteristics that could explain differences in habitat and abundance: (i) intraspecific variation in dormancy level; (ii) germination response to different light conditions; (iii) light and temperature interactions at germination; (iv) timing of seedling emergence; and (v) seed persistence in soil. Bromus sterilis and B. tectorum behaved similarly in all tests. For both these species, there were large differences in dormancy level among populations and strong inhibition of germination by light. In addition, emergence from seeds sown on the soil surface was both delayed and reduced compared with buried seeds. In contrast, B. hordeaceus and B. arvensis showed generally weak dormancy, and germination was only slightly inhibited by light. It was concluded that germination characteristics alone do not explain the differences in weediness between these four species.